Administration of nerve growth factor-β to heifers with a pre-ovulatory follicle enhanced luteal formation and function and promoted LH release

被引:9
|
作者
Stewart, Jamie L. [1 ,4 ]
Stella, Stephanie [1 ]
Cunha, Lais L. [1 ]
Dias, Nicholas W. [2 ]
Canisso, Igor F. [1 ]
Mercadante, Vitor R. G. [2 ]
Cardoso, Rodolfo C. [3 ]
Williams, Gary L. [3 ]
Pohler, Ky G. [3 ]
Lima, Fabio S. [1 ,5 ]
机构
[1] Univ Illinois, Coll Vet Med, Dept Vet Clin Med, Urbana, IL 61801 USA
[2] Virginia Polytech Inst & State Univ, Dept Anim & Poultry Sci, Blacksburg, VA 24061 USA
[3] Texas A&M Univ, Dept Anim Sci, College Stn, TX 77843 USA
[4] Virginia Polytech Inst & State Univ, Dept Large Anim Clin Sci, Virginia Maryland Coll Vet Med, Blacksburg, VA 24061 USA
[5] Univ Calif Davis, Sch Vet Med, Dept Populat Hlth & Reprod, Davis, CA 95616 USA
基金
美国食品与农业研究所;
关键词
NGF; Luteinizing hormone; Ovulation; Progesterone; OVULATION-INDUCING FACTOR; SEMINAL PLASMA; CORPUS-LUTEUM; GENE-EXPRESSION; ESTROUS-CYCLE; BLOOD-FLOW; PROGESTERONE PRODUCTION; EMBRYO DEVELOPMENT; OVARIAN-FUNCTION; STAR PROTEIN;
D O I
10.1016/j.theriogenology.2020.02.040
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The objective of this study was to determine the effects of bovine nerve growth factor-beta (NGF) on pre-ovulatory follicle vascular area, LH release, ovulation, and luteal function when administered systemically to heifers. Post-pubertal Holstein heifers (n = 12) received an intravaginal progesterone-releasing device (CIDR) and GnRH agonist (100 mu g IM). The CIDR was removed 5 d later, and heifers were given dinoprost (25 mg IM) at CIDR removal and 24 h later, followed by a second dose of GnRH agonist 48 h later. Heifers were randomly assigned to treatments using a cross-over design. For example, heifers assigned to NGF (250 mu g reconstituted in 12 mL PBS IM) in replicate 1 were assigned to control (12 mL PBS IM) in replicate 2. Transrectal ultrasonography was performed before treatment and repeated every 4 h up to 32 h to determine the pre-ovulatory follicle diameter, vascular area, and ovulation. Serum samples were obtained to assess LH concentrations during the periovulatory period and every 2 d post-ovulation for measuring progesterone concentrations. A subset of heifers had luteal biopsies performed on days 9 (n = 6 per treatment) and 14 (n = 6 per treatment) post-ovulation to count luteal cell numbers and measure relative mRNA abundance for steroidogenic and angiogenic enzymes and LH receptor. Treatment with NGF increased pre-ovulatory follicle diameter (P = 0.02) and serum LH concentrations (P = 0.03) but did not affect time to ovulation (P = 0.42). Heifers treated with NGF had increased serum progesterone concentrations in the subsequent luteal phase (P = 0.03), but no change in vascular area of the follicle (P = 0.16) or CL (P = 0.20). Heifers treated with NGF had a greater number of small luteal cells (P < 0.01) and a tendency for increased LH receptor (LHR) mRNA abundance in the CL (P = 0.10). There was also increased steroidogenic acute regulatory protein (STAR; P = 0.05) and a tendency for increased cytochrome P450 family 11 (CYP11A1; P = 0.10) mRNA abundance in the CL of NGF-treated heifers. There was decreased prostaglandin E-2 synthase (PGES; P = 0.03) and its receptor (PGER; P = 0.05) mRNA abundance and a tendency for decreased cytochrome P450 family 17 subfamily A member 1 (CYP17A1; P = 0.08) and hydroxysteroid 17-beta dehydrogenase (HSD17B; P = 0.06) mRNA abundance in the CL of NGF-treated heifers. Administration of NGF improved CL function in heifers potentially as a result of increased LH release. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:37 / 47
页数:11
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